Anesthesia Kit

What Is This Device?

This product code has been established in accordance with the may 20, 1997, guidance entitled, convenience kits interim regulatory guidance, found at www.Fda.Gov/cdrh/ode/convkit.Html. This type of convenience kit, as listed in the guidance above, is under enforcement discretion, and does not require a premarket notification (510(k)) to market if it meets all criteria in the guidance.

What Is FDA Product Code OFQ?

Anesthesia Kit is FDA product code OFQ, Class 2, 21 CFR 868.5120.

How Does It Reach the US Market?

The FDA exercises enforcement discretion for this code and does not currently require a premarket submission for devices that meet the conditions it has set for it.

What Do the Recalls Say?

The FDA has recorded 8 recalls under this product code since 2022. None was by a company in China. 1 is Class I, the most serious grade.

The root causes the FDA records most often are Nonconforming Material/Component (3), Process change control (1) and Device Design (1). A recall is a fact about one product and its maker, not a grade for every manufacturer of the type.